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TPM2, tropomyosin 2

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TPM2, tropomyosin 2

  • This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]

  • Gene Synonyms (tropomyosin beta chain, epididymis secretory protein Li 273, nemaline myopathy type 4, tropomyosin 2 (beta), AMCD1, DA1, DA2B, DA2B4, HEL-S-273, NEM4, TMSB,)
  • NCBI Gene ID: 7169
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q5TCU3
    UNIPROT ID#>>A7XZE4
    UNIPROT ID#>>V9HW25
    UNIPROT ID#>>P07951
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

tropomyosin 2 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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